Philips Electronics North America recalls

Philips Electronics North America appears in 163 official U.S. recall notices indexed by RecallRadar.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• HeartStart MRx Monitor/Defibrillator Models: M3535A and M3536A
  FDA Device · Class II · 2016-09-28 · Philips Electronics North America
• UNIQ 1.0: UNIQ FD10, 722026
  FDA Device · Class II · 2016-09-07 · Philips Electronics North America
• Allura Xper with release R8.2: Allura Xper FD10, 722026
  FDA Device · Class II · 2016-09-07 · Philips Electronics North America
• Philips DuraDiagnost stationary X-ray system
  FDA Device · Class II · 2016-09-07 · Philips Electronics North America
• PCR Compano Basic Reader using 100-127V as mains voltage
  FDA Device · Class II · 2016-09-07 · Philips Electronics North America
• MultiDiagnost Eleva with Flat Detector
  FDA Device · Class II · 2016-08-10 · Philips Electronics North America
• UroDiagnost
  FDA Device · Class II · 2016-08-10 · Philips Electronics North America
• MultiDiagnost Eleva
  FDA Device · Class II · 2016-08-10 · Philips Electronics North America
• IntelliVue Patient Monitor Product Usage: The monitors are indicated for use by health care professionals whenever there is a need for moni…
  FDA Device · Class II · 2016-08-10 · Philips Electronics North America
• HeartStart MRx Monitor/Defibrillator The HeartStart MRx is for use for the termination of ventricular tachycardia and ventricular fibrillat…
  FDA Device · Class II · 2016-05-11 · Philips Electronics North America
• eValueMed Infant Transport Mattress 301-1015, Distributed by Tri-anima A disposable heel warmer for use when circulation needs to be stimul…
  FDA Device · Class II · 2016-04-13 · Philips Electronics North America
• evaluemed Infant Heel Warmer 301-1223
  FDA Device · Class II · 2016-04-13 · Philips Electronics North America
• Philips X-Ray Systems, Allura Xper with R8.2.16 Product Usage: The Allura Xper FD1O and Allura Xper FD1O/10 is intended for use in cardiova…
  FDA Device · Class II · 2016-03-16 · Philips Electronics North America
• SENSE Body Coil 1.5T with identification
  FDA Device · Class II · 2016-03-09 · Philips Electronics North America
• Philips IntelliVue Measurement Module X1 Model: M3001A
  FDA Device · Class II · 2016-03-02 · Philips Electronics North America
• Philips Healthcare IntelliVue Info Center iX, A.0 866023
  FDA Device · Class II · 2016-03-02 · Philips Electronics North America
• Philips IntelliVue Module Measurement X2 Model: M3002A
  FDA Device · Class II · 2016-03-02 · Philips Electronics North America
• Philips Healthcare IntelliVue Info Center iX, B.0, 866389 Physiological, Patient Monitor (With Arrhythmia Detection or Alarm)
  FDA Device · Class II · 2016-03-02 · Philips Electronics North America
• Philips Healthcare PIIC Classic Upgrade, 866117 Physiological, Patient Monitor (With Arrhythmia Detection or Alarm)
  FDA Device · Class II · 2016-03-02 · Philips Electronics North America
• Actuator for angiographic x-ray monitor ceiling suspension system
  FDA Device · Class II · 2016-02-24 · Philips Electronics North America
• Allura Xper FD OR Table, Ceiling version only
  FDA Device · Class II · 2016-02-17 · Philips Electronics North America
• Philips Allura Xper FD20 Ceiling version only
  FDA Device · Class II · 2016-02-17 · Philips Electronics North America
• Philips Healthcare TraumaDiagnost
  FDA Device · Class II · 2016-02-17 · Philips Electronics North America
• INTEGRIS V3000
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS BV3000 MONO
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD20/20
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• UNIQ FD
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD10, FD10 C, and FD10 F
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD10/10
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• UNIQ FD OR table
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura CV20
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS V5000: Model Number: 72248 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neur…
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS Allura 15-12 (biplane)
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Cardiovascular Allura Centron
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS BV5000: Model Number: 72249 The Philips INTEGRIS 3000 I 5000 system is intended for interventional and diagnostic vascular and neu…
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD20/10
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD20 OR Table
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD20
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS BH5000
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS Allura 9 (biplane)
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS H5000
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD20/15
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS BN/BV3000
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD20 Biplane OR Table
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD20/20 OR Table
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD20 Biplane
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• Allura Xper FD10 OR Table
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS H3000
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS BH3000
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America
• INTEGRIS CV
  FDA Device · Class II · 2016-02-10 · Philips Electronics North America